孟德尔随机化
子宫肌瘤
更年期
全基因组关联研究
医学
平滑肌瘤
妇科
生物
睾酮(贴片)
生理学
产科
子宫
内科学
遗传学
单核苷酸多态性
基因
病理
遗传变异
基因型
作者
Hefei Wang,Chun Li,Lanlan Chen,Mengwen Zhang,Tong Ren,Songling Zhang
标识
DOI:10.1016/j.rbmo.2023.103584
摘要
Abstract
Research question
Are the observed associations between female reproductive factors and sex hormones with the risk of uterine leiomyoma truly causal associations? Design
The putative causal relationships between female reproductive factors and sex hormones with uterine leiomyoma were investigated using two-sample Mendelian randomization. Statistics on exposure-associated genetic variants were obtained from genome-wide association studies (GWAS). The uterine leiomyoma GWAS from the FinnGen and FibroGENE consortia were used as outcome data for discovery and replication analyses, respectively. Results were pooled by meta-analysis. Sensitivity analyses ensured robustness of the Mendelian randomization analysis. Results
When FinnGen GWAS were used as outcome data, a causal relationship was found between age at menarche (OR 0.84, P < 0.0001), age at menopause (OR 1.08, P < 0.0001), number of live births (OR 0.25, P < 0.001) and total testosterone levels (OR 0.90, P < 0.001) with the risk of uterine leiomyoma. When FibroGENE GWAS were used as outcome data, Mendelian randomization results for age at menopause, the number of live births and total testosterone levels were replicated. In the meta-analysis, a later age at menopause (OR 1.08, P < 0.0001) was associated with an increased risk of uterine leiomyoma. A higher number of live births (OR 0.25, P < 0.0001) and higher total testosterone levels (OR 0.90, P < 0.0001) were associated with a decreased risk of uterine leiomyoma. Conclusions
A causal relationship between later age at menopause, lower number of live births and lower total testosterone levels with increased risk of uterine leiomyoma was found.
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